Distal end for ligating band dispenser

ABSTRACT

A supporting structure for a ligating band dispensing device adapted to be coupled to a distal end of an endoscope comprises a rigid substantially cylindrical, transparent outer support surface adapted to receive a plurality of ligating bands thereon, wherein the support surface includes a distal portion extending from a distal end thereof proximally to a distal-most ligating band receiving area. A channel extends axially through the support surface from the distal end to a proximal end thereof, wherein an abutting surface is formed along at least a portion of a circumference of the channel to define a distal-most point of penetration of an endoscope received therein. A gripping surface extending around at least a portion of a circumference of the proximal end of the channel is sized so that, when an endoscope extends into the proximal end of the channel, the gripping surface frictionally couples the support surface to the endoscope.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation of application Ser. No. 09/544,590,filed Apr. 6, 2000, now U.S. Pat. No. 6,610,070 which is a Continuationof application Ser. No. 09/220,477, filed Dec. 23, 1998, now U.S. Pat.No. 6,059,798, which is a Continuation of application Ser. No.08/869,055, filed Jun. 4, 1997, now U.S. Pat. No. 5,853,416, all ofwhich are incorporated in their entirety by reference herein.

FIELD OF THE INVENTION

The invention relates generally to the field of tissue ligation, andmore particularly to an improved distal end for a device for dispensingligating bands.

BACKGROUND OF THE INVENTION

Physicians have used elastic ligating bands to treat lesions, includinginternal hemorrhoids and mucositis and for performing mechanicalhemostasis. The object of such ligation is to position a ligating band,which is usually elastic, over the targeted lesion or blood vesselsection by first stretching the band beyond its undeformed diameter andthen drawing the tissue to be ligated within the band. Thereafter theband is released so that it contracts, applying inward pressure on thesection of tissue caught within the band. The effect of the inwardpressure applied by the band is to stop all circulation through thetargeted tissue, thereby causing the tissue to die. The body thensloughs off the dead tissue or the dead tissue may be aspirated into anendoscope or a similar device.

U.S. Pat. No. 5,398,844 to Zaslavsky et al. (“the Zaslavsky patent”),which is incorporated herein by reference, describes a ligating banddispensing device including a substantially cylindrical support surfaceover which elastic ligating bands are stretched. The cylindrical supportsurface is typically attached to the distal end of an endoscope which isadvanced into the body to a target area. A user then applies suctionthrough the endoscope to draw the tissue to be ligated into thecylindrical support surface and releases a ligating band to contractaround the tissue.

Previous ligating band dispensers allowed a user to dispense only asingle ligating band at a time. That is, after a single ligating bandwas dispensed, if a user wanted to ligate another portion of tissue, theuser would remove the device from the patient's body, load a newligating band on the device and reinsert the device to the desired areawithin the patient's body. The device of the Zaslavsky patent, allows auser to place several ligating bands at desired locations withoutremoving the device from the patient's body to reload ligating bands.However, as the number of ligating bands included on the distal end ofthese devices has been increased, the field of vision from theendoscopes to which these devices are normally coupled has beencorrespondingly decreased.

More specifically, as shown in FIGS. 1 and 2 a known support surface 2around which several elastic ligating bands 4 are received is mounted onthe distal end of an endoscope 6. This support surface 2 is preferablyformed of a rigid material, for example polycarbonate. The rigidity ofthis support surface 2 is necessary to maintain the size of the distalopening of the support surface 2 as the support surface 2 is subjectedto compressive forces from the ligating bands 4 and from vacuum pressureused to draw tissue into a tissue receiving space 18 formed axiallythrough the support surface 30. A proximal end of the support surface 2is coupled to an elastic ring 8 formed of, for example, silicone. Theelastic ring 8 grips the distal end of the endoscope 6 to frictionallycouple the support surface 2 to the endoscope 6. A shoulder 10 formed atthe juncture between the support surface 2 and the ring 8 maintains apredetermined separation between the distal-most surface 12 of theendoscope 6 and the distal end 14 of the support surface 2 to provide aspace 18 within which the tissue to be ligated may be received. Thespace 18 is often substantially conical with a minimum diameter at aproximal end thereof of, for example, 0.375 inches and a maximumdiameter at the distal end of the support surface of 0.5 inches. As theendoscope 6 is received only within the elastic ring 8 and does notextend into the rigid support surface 2, this support surface 2 may becoupled to endoscopes 6 of various diameters with no modification.

FIGS. 3 and 4 show cross-sectional views of other known support surfaces2′ and 2″, each also being adapted to receive an endoscope so that thedistal end 12 of the endoscope 6 abuts a proximal end surface 7 of thesupport surface 30. The distal end 12 of the endoscope 6 is receivedwithin the ring 8 but does not extend into the support surface 30. Thespace 18 within the support surface 2, which is of substantially uniformdiameter throughout, is reserved only for receiving the tissue to beligated. This is true for both the 8 ligating band receiving supportingsurface 2′ and the 5 ligating band receiving support surface 2″.

Even if the support surface 2 is made of transparent material, thebreadth of the visual field of an optical device 16 (shown by the dottedlines in FIG. 2) included in the endoscope 6 is limited by the extent towhich the ligating bands 4 extend distally of the distal end 12 of theendoscope 6. And, as the number of ligating bands 4 is increased, thedistal extension of the ligating bands 4 is also increased, resulting ina corresponding decrease in the extent of the visual field.

SUMMARY OF THE INVENTION

The present invention is directed to a supporting structure for aligating band dispensing device being adapted to be coupled to a distalend of an endoscope. The supporting structure comprises a rigidsubstantially cylindrical, transparent support surface adapted toreceive a plurality of ligating bands thereon, wherein the supportsurface includes a distal portion extending from a distal end thereofproximally to a distal-most ligating band receiving area. A channelextends axially through the support surface from the distal end to aproximal end thereof and an abutting surface formed along at least aportion of a circumference of the channel defines a distal-most point ofpenetration of an endoscope received within the channel. A grippingsurface, extending around at least a portion of a circumference of theproximal end of the channel sized so that, when an endoscope extendsinto the proximal end of the channel, the gripping surface frictionallycouples the support surface to the endoscope.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be more readily understood through the followingdetailed description, with reference to the accompanying drawings, inwhich:

FIG. 1 is a perspective view of a known distal end of a ligating banddispensing device;

FIG. 2 is a cross-sectional view of the ligating band dispensing deviceof FIG. 1, taken along line 2—2 of FIG. 1;

FIG. 3 is a cross-sectional view of a second prior art support surface;

FIG. 4 is a cross-sectional view of a third prior art support surface;

FIG. 5 is a perspective view of a distal end of a ligating banddispensing device according to a first embodiment of the presentinvention;

FIG. 6 is a cross-sectional view of the ligating band dispensing deviceof FIG. 5, taken along line 4—4 of FIG. 5;

FIG. 7 is a cross-sectional view of a ligating dispensing deviceaccording to a second embodiment of the invention; and

FIG. 8 is a cross-sectional view of a ligating dispensing deviceaccording to a third embodiment of the invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

As illustrated in FIG. 5, a device 1 according to a first embodiment ofthe present invention includes a substantially cylindrical supportsurface 30 coupled to an elastic ring 8. A central bore 3 which extendsthrough the support surface 2 and the elastic ring 8, in operation,receives the distal end of an endoscope 6. A plurality (8 in this case)of ligating bands 4 are received around the support surface 30 with atrigger line 20 wrapping around each of the ligating bands 4 in arepeating pattern. The support surface 30 and the support surface 30′ ofFIG. 7 for receiving 8 ligating bands 4 thereon will preferably bebetween 0.5 and 0.8 inches in length and may preferably be between 0.65and 0.75 inches in length. While the support surface 30″ of FIG. 8 maypreferably be between 0.45 and 0.65 inches in length and is morepreferably between 0.5 and 0.6 inches in length. Of course, thoseskilled in the art will understand that the length of the supportsurface may need to be varied depending on the thickness of the ligatingbands (in a direction distal to proximal) received thereon. The ligatingbands 4 are received on the support surface 30 so that a distal-mostband 4 is separated from a distal end 14 of the support surface 30 by anarea 15 which is, except for the trigger line 20, substantially freefrom visual obstructions. The support surface 30 is preferablysubstantially transparent. However, those skilled in the art willunderstand that at least the area 15, which preferably extends 0.2–0.3″should be transparent.

The trigger line 20 extends from a proximal end accessible to a user,through a lumen 22 in the endoscope 6 to pass through the centralbore 3and out to the support surface 30 via a first one of a plurality ofgrooves 24. The trigger line 20 then extends across the support surface2, passes over the distal-most of the ligating bands 4 and wrapsunderneath this ligating band 4 to extend back into the first groove 24.The trigger line 20 then loops under the distal end 14 of the supportsurface 30 and passes through a second groove 24 adjacent to the firstgroove, passes under the distal-most band 4, wraps around this band 4and passes under and around a second band immediately proximal to thedistal-most band 4. The trigger line 20 continues over the second band 4and passes back under the distal-most band 4 to extend to the secondgroove 24, returning from the second groove 24 to wrap over and aroundthe second band 4, under the third band 4, etc. This pattern is repeateduntil the trigger line 20 extends around each of the ligating bands 4received on the support surface 30. Of course, the arrangement of thetrigger line 20 may be varied substantially so long as it is arranged sothat a user is permitted to release each of the plurality of ligatingbands 4 one at a time at each of a corresponding plurality of locationswithin the patient. Thus, for example, a separate trigger line 20 may beprovided for each of the ligating bands 4 or a single line 20 may bedivided at some point between the user and the support surface 30 into aplurality of filaments each of which is coupled to a respective ligatingband 4.

The endoscope 6 extends past the juncture between the ring 8 and thesupport surface 30 to a shoulder 10 formed at a portion of the centralbore 3 within the support surface 30. This shoulder 10 may preferably belocated beneath one of the distal-most of the ligating bands 4 and ismost preferably located so that, prior to releasing any ligating bands,the shoulder is beneath the third ligating band (counting distal toproximal) preferably between 0.35 and 0.5″, and more preferablyapproximately 0.38″ from the distal end of the support surface 30. Thisshoulder 10 prevents the endoscope 6 from moving past a distal-mostposition within the central bore 3, to create a substantiallyunobstructed space 18 extending from the distal end 14 proximally to thedistal end of the endoscope 6. This space 18, which is dimensionedsimilarly to that of the support surface 2 described above, is separatedat the shoulder 10 from an increased diameter endoscope receivingportion 31 of the bore 3 which preferably has a diameter of between 0.4and 0.5 inches depending upon the diameter of the endoscope 6 which isto be received therein. The space 18 provides an area into which tissueto be ligated may be drawn so that a ligating band 4 released from thesupport surface 30 will encircle and grip the tissue to the extentnecessary for the band 4 to be maintained in position on the tissueafter the tissue has been released. That is, the tissue is drawn intothe space 18 by known means such as, for example suction or a grippingmechanism (not shown) provided via the lumen 22. Thus, the placement ofthe endoscope 6 within the rigid support surface 30 and the extension ofthe support surface 30 distally beyond the distal-most ligating band 4allow the space 18 to extend distally of the distal-most band 4.

As noted above, the distal end of the endoscope 6 includes an opticaldevice 16 and a light source 26 which allow a user to view the areaadjacent to the distal end of the device 1. The placement of theendoscope 6 within the rigid support surface 30 and the consequentplacement of the tissue receiving space 18 distally toward thedistal-most band 4 (or distally past all of the ligating bands 4),allows the field of vision of the optical device 16 (shown by the dottedlines in FIG. 6) to be increased relative to that obtained with anendoscope 6 seated proximal to the juncture between the ring 8 and thesupport surface 30. Those skilled in the art will understand that anincrease of nearly 2 to 1 over prior placement positions of theendoscope may be obtained with this arrangement. Of course, thisincrease of the field of vision is achieved only when the supportsurface 30 is formed of a transparent material which may preferably bepolycarbonate.

As described above, the elastic ring 8 of the support surface 30 gripsthe endoscope 6 to prevent if from becoming separated from the supportsurface 30. However, those skilled in the art will understand that inorder to maintain a proper fit of the endoscope 6 within the rigidsupport surface 2, or to accommodate larger endoscopes 6, sizing theendoscope receiving portion 31 of the central bore 3 to correspond tothe diameter of the distal end of a particular endoscope 6 will providea more secure and stable mating with the support surface 30.

In operation, a plurality of ligating bands 4 are placed on the supportsurface 30 with the trigger line 20 threaded between the bands 4 asdescribed above. Then an endoscope 6 is passed into the endoscopereceiving portion 31 of the central bore 3 via an opening formed in theproximal end of the elastic ring 8 until a distal end of the endoscope 6contacts the shoulder 10 and the trigger line 20 extended from theproximal end of the endoscope 6 through the central bore 3 to theligating bands 4 (preferably via the lumen 22). The endoscope 6 is theninserted into a patient and advanced, under visual observation (viaoptical device 16) until the distal end 14 of the support surface 30 isadjacent to a portion of tissue to be ligated. The user then draws thetissue into the space 18 by, for example, advancing a gripping device(not shown) through the lumen 22 and grasping the tissue, or by applyingsuction through the lumen 22. When the tissue is in a desired positionwithin the space 18, a user draws the trigger line 20 proximally throughthe lumen 22 until the distal-most ligating band 4 is released from thesupport surface 30 to ligate the tissue. As described in the Zaslavskypatent, the trigger mechanism of a ligating device incorporating asupport surface according to the present invention will preferablyprovide the user with a tactile indication that a band 4 has beenreleased. Thereafter, the user releases the tissue by withdrawing thegripping device or stopping application of the vacuum pressure and thenvisually guides the endoscope 6 to a second location within the patient.When the support surface 30 is located adjacent to a second portion oftissue to be ligated, the user repeats the process described above,releasing a second of the plurality of ligating bands 4. The second ofthe plurality of ligating bands 4 is preferably, after release of thefirst of the plurality of ligating bands 4, the distal-most ligatingband 4 received on the support surface. The remaining ligating bands 4may then be released one at a time, starting with the distal-mostremaining ligating band 4 and progressing to the proximal-most band 4.Thus, the device 1 allows a user to ligate 8 or more portions of tissuewithout removing the device 1 from the patient while providing the userwith improved control of the endoscope 6 resulting from the expandedvisual field.

The support surface 30″ of FIG. 8 differs from the support surfaces 30and 30′ only in that it is shorter as it is intended to receive only 5ligating bands thereon. Of course, those skilled in the art willunderstand that increased numbers of ligating bands 4 may be received ona support surface as described simply by lengthening the endoscopereceiving portion 31 of support surface to the extent that the increasein length of the support surface does not result in excessive irritationto the patient or to difficulties in inserting the device into a bodylumen.

There are many modifications of the disclosed embodiments which will beapparent to those of skill in the art. It is understood that thesemodifications are within the teaching of the invention which is to belimited only by the claims appended hereto.

1. A ligating band dispensing device having a supporting structurelocated at a distal end of the ligating band dispensing device, thesupporting structure comprising: a rigid support surface having a firstportion that extends proximally from a distal end of the supportingstructure to a distal-most ligating band receiving area and a secondportion that extends proximally from the distal-most ligating bandreceiving area; a plurality of elastic ligating bands received aroundthe second portion of the rigid support surface; and a channel extendingaxially through the supporting structure; wherein at least the firstportion of the rigid support surface is substantially transparent; andwherein the supporting structure further comprises position fixing meansdefining a distal-most point of penetration of a distal end of anendoscope received in the channel wherein the position fixing means islocated distally of a proximal-most one of the ligating bands.
 2. Theligating band dispensing device according to claim 1, wherein theposition fixing means includes an endoscope abutting surface extendinginto the channel.
 3. The ligating band dispensing device according toclaim 2, wherein the endoscope abutting surface projects radially intothe channel and extends around at least a portion of the channel.
 4. Theligating band dispensing device according to claim 1, wherein the rigidsupport surface extends at least 0.5″ from the distal end to theproximal end thereof.
 5. A ligating band dispensing device having asupporting structure located at a distal end of the ligating banddispensing device, the supporting structure comprising: a rigid supportsurface having a first portion that extends proximally from a distal endof the supporting structure to a distal-most ligating band receivingarea and a second portion that extends proximally from the distal-mostligating band receiving area; a plurality of elastic ligating bandsreceived around the second portion of the rigid support surface; and achannel extending axially through the supporting structure; wherein atleast the first portion of the rigid support surface is substantiallytransparent; and wherein the distal end of the rigid support surfaceincludes a plurality of grooves formed therein for receiving a triggerline.
 6. The ligating band dispensing device according to claim 2,wherein the abutting surface is substantially aligned with thedistal-most ligating band.
 7. The ligating band dispensing deviceaccording to claim 5, wherein the supporting structure further comprisesposition fixing means defining a distal-most point of penetration of adistal end of an endoscope received in the channel wherein the positionfixing means is located distally of a proximal-most one of the ligatingbands.
 8. The ligating band dispensing device according to claim 5,wherein the supporting structure further comprises an abutting surfacedefining a distal-most point of penetration of a distal end of anendoscope received in the channel wherein the abutting surface islocated distally of a proximal-most one of the ligating bands.
 9. Theligating band dispensing device according to claim 8, wherein theabutting surface projects radially into the channel and extends aroundat least a portion of the channel.
 10. The ligating band dispensingdevice according to claim 8, wherein the abutting surface issubstantially aligned with the distal-most ligating band.